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Results 1 - 10 of 83 for Congenital blindness
  1. Autosomal recessive congenital stationary night blindness 
    Autosomal recessive congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
  2. Autosomal dominant congenital stationary night blindness 
    ... Kraft TW, Gross AK. 1 rhodopsin mutations in congenital night blindness. Adv Exp Med Biol. 2010;664:263-72. ...
    https://medlineplus.gov/...ant-congenital-stationary-night-blindness - Genetics
  3. X-linked congenital stationary night blindness 
    X-linked congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light and ...
    https://medlineplus.gov/...ked-congenital-stationary-night-blindness - Genetics
  4. Leber congenital amaurosis 
    ... Amaurosis, Leber congenital Congenital amaurosis of retinal origin Congenital retinal blindness CRB Dysgenesis neuroepithelialis retinae Hereditary epithelial dysplasia of ...
    https://medlineplus.gov/.../condition/leber-congenital-amaurosis - Genetics
  5. RHO gene 
    ... Kraft TW, Gross AK. 1 rhodopsin mutations in congenital night blindness. Adv Exp Med Biol. 2010;664:263-72. ...
    https://medlineplus.gov/genetics/gene/rho - Genetics
  6. CACNA1F gene 
    ... have been identified in people with X-linked congenital stationary night blindness. Mutations in this gene are responsible for the ... vision problems similar to those of X-linked congenital stationary night blindness.Researchers have identified at least one CACNA1F mutation ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  7. NYX gene 
    ... have been identified in people with X-linked congenital stationary night blindness. Mutations in this gene are responsible for the ... the other vision problems characteristic of X-linked congenital stationary night blindness. The mutations responsible for high myopia each change ...
    https://medlineplus.gov/genetics/gene/nyx - Genetics
  8. TRPM1 gene 
    ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009 Nov;85(5): ...
    https://medlineplus.gov/genetics/gene/trpm1 - Genetics
  9. GRM6 gene 
    ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... coupling in an mGluR6 point mutant associated with congenital stationary night blindness. Mol Pharmacol. 2009 Nov;76(5):992-7. ...
    https://medlineplus.gov/genetics/gene/grm6 - Genetics
  10. PDE6B gene 
    ... gene has been found to cause autosomal dominant congenital stationary night blindness, which is characterized by the inability to see ... Artemyev NO. Mutation in rod PDE6 linked to congenital stationary night blindness impairs the enzyme inhibition by its gamma-subunit. ...
    https://medlineplus.gov/genetics/gene/pde6b - Genetics
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